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49525

Sigma-Aldrich

L-Glutamic acid γ-(3-carboxy-4-nitroanilide) ammonium salt

≥99.0% (TLC)

Synonym(s):

L-Glutamic acid 5-(3-carboxy-4-nitroanilide) ammonium salt

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About This Item

Linear Formula:
C12H12N3O7NH4
CAS Number:
63699-78-5
Molecular Weight:
328.28
EC Number:
264-418-7
MDL number:
MFCD00058243
UNSPSC Code:
12352204
PubChem Substance ID:
57651202
NACRES:
NA.77

Quality Level

200

Assay

≥99.0% (TLC)

form

powder

impurities

≤6% water

solubility

H2O: 100 mg/mL, clear, yellow-green

suitability

suitable as substrate for γ-glutamyltranspeptidase test

storage temp.

2-8°C

SMILES string

N.N[C@@H](CCC(=O)Nc1ccc(c(c1)C(O)=O)[N+]([O-])=O)C(O)=O

InChI

1S/C12H13N3O7.H3N/c13-8(12(19)20)2-4-10(16)14-6-1-3-9(15(21)22)7(5-6)11(17)18;/h1,3,5,8H,2,4,13H2,(H,14,16)(H,17,18)(H,19,20);1H3/t8-;/m0./s1

InChI key

GFABNNMTRVBLPZ-QRPNPIFTSA-N

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Application

L-Glutamic acid γ-(3-carboxy-4-nitroanilide) ammonium salt has been used as a synthetic substrate for gamma-glutamyltransferase (GGT) to determine GGT activity.

Other Notes

Substrate for γ-glutamyl transferase

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM2785
BCCM5748
BCCK3114
BCCJ4893
BCCH3579

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L M Shaw et al.
Clinical chemistry, 23(1), 79-85 (1977-01-01)
The kinetics of human serum gamma-glutamyltransferase (EC 2.3.2.2) were investigated, with use of glycylglycine as a gamma-glutamyl acceptor substrate and gamma-glutamyl-4-nitroanilide and its carboxy derivative, gamma-glutamyl-3-carboxy-4-nitroanilide, as donor substrates. The simultaneous occurrence of both gamma-glutamyltransfer and autotransfer was established by
A kinetic study of gamma-glutamyltransferase (GGT)-mediated S-nitrosoglutathione catabolism.
Angeli V
Archives of Biochemistry and Biophysics, 481(2), 191-196 (2009)

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